Package 0220-4835-41

Brand: sulphur iodatum

Generic: sulfur iodide
NDC Package

Package Facts

Identity

Package NDC 0220-4835-41
Digits Only 0220483541
Product NDC 0220-4835
Description

12 [hp_C] in 1 TUBE (0220-4835-41)

Marketing

Marketing Status
Marketed Since 1983-03-03
Brand sulphur iodatum
Generic sulfur iodide
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0a3400ec-70d1-340c-e063-6394a90ad39d", "openfda": {"unii": ["L6L8KA2AA0"], "spl_set_id": ["8693d143-14d1-5272-e053-2991aa0a2e6c"], "manufacturer_name": ["Boiron"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "12 [hp_C] in 1 TUBE (0220-4835-41)", "package_ndc": "0220-4835-41", "marketing_start_date": "19830303"}], "brand_name": "Sulphur iodatum", "product_id": "0220-4835_0a3400ec-70d1-340c-e063-6394a90ad39d", "dosage_form": "PELLET", "product_ndc": "0220-4835", "generic_name": "SULFUR IODIDE", "labeler_name": "Boiron", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Sulphur iodatum", "active_ingredients": [{"name": "SULFUR IODIDE", "strength": "12 [hp_C]/12[hp_C]"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "19830303", "listing_expiration_date": "20261231"}